A number of ClLlabelled compounds were fed to detached leafy twigs of Colorado spruce (Picen pz~ngens Engelm.), and after a metabolic period of 24 hours the pungenin was isolated and the specified activities of the glucose lnqiety and the aglycone (3,4-dihydroxyacetophenone) were determined. 111 some Instances the aglycone was degraded further to determine the C1" in the methyl and carbonyl carbons separately.Caffeic acid and L-phenylalanine were the best precursors of the aglycone; cinnamic acid, 9-coumaric acid, phenyllactic acid, and shikimic acid were quite good. Sodium acetate was a poor precursor, and was converted to glucose more readily than to the aglycone. Compounds found to be very poor precursors include tyrosine, 3,4-dihydroxyphenylalanine, 3-hydroxytyramine, phenylacetic acid, mandelic acid, 9-hydrosyphenylpyr~~vic acid, 9-hydroxyphenyllactic acid, p-hydrosybenzoic acid, and protocatechuic acid. Cinnarnic acid-a-Cll gave 3,4-dihydroxyacetophenone labelled chiefly in the methyl group, while cinnamic acid-P-Cl", ~-phenylalanine-P-C1~~, 9-couinaric acid-P-Cl", and carfeic acid-P-C1.1 formed 3,4-dihydrosyacetophenone labelled mainly in the carbonyl carbon. I t appears that a phenylethanoid compound is formed by a process involving the loss of the terminal carbon of a phenylpropanoid co~npound.3,4-Dihydroxyacetophenone-carbonyl-CN was fed t o spruce twigs bearing new terminal growth; up t o 20% was converted to pungenin but most of it formed unidentified compounds. I t was a poor precursor of lignin, compared with cinnamic acid, and a poor precursor of glutamic acid, relative to acetate.'Manuscript